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In silico analysis of single nucleotide polymorphisms (SNPs) in human FOXC2 gene
Introduction: Lymphedema is an abnormal accumulation of interstitial fluid, due to inefficient uptake and reduced flow, leading to swelling and disability, mostly in the extremities. Hereditary lymphedema usually occurs as an autosomal dominant trait with allelic heterogeneity. Methods: We identifie...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | F1000Res |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
F1000 Research Limited
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5814747/ https://ncbi.nlm.nih.gov/pubmed/29511529 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.10937.2 |
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